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Reliability of panel-based mutational signatures for immune-checkpoint-inhibition efficacy prediction in non-small cell lung cancer

Lung cancer (Amsterdam, Netherlands), 2023-08, Vol.182, p.107286-107286, Article 107286

2023

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Targeted next‐generation sequencing using a multigene panel in myeloid neoplasms: Implementation in clinical diagnostics

International journal of laboratory hematology, 2017-12, Vol.39 (6), p.604-612

2017

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Gezamenlijke reflectie over ethische twijfel met CURA: een laagdrempelig instrument voor moreel beraad

Tijdschrift voor geneeskunde, 2024-03

2024

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Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

Human reproduction (Oxford), 2010-12, Vol.25 (12), p.3159-3160

2010

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Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map

Journal of medical genetics, 2004-09, Vol.41 (9), p.691-698

2004

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Novel PORCN mutations in focal dermal hypoplasia

Clinical genetics, 2009-12, Vol.76 (6), p.535-543

2009

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Sporadic male patients with intellectual disability: Contribution of X-chromosome copy number variants

European journal of medical genetics, 2012-11, Vol.55 (11), p.577-585

2012

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Digitale werktuigkist met ethische overlegmethoden in de zorg

Tijdschrift voor geneeskunde, 2024-04

2024

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High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation

Journal of medical genetics, 2008-07, Vol.45 (7), p.447-450

2008

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Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males

American journal of human genetics, 2005-09, Vol.77 (3), p.442-453

2005

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X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms

Clinical genetics, 2002-12, Vol.62 (6), p.423-432

2002

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1037P Tumour mutational burden and HLA diversity by TruSight oncology 500 (TSO500) next generation sequencing panel and clinical outcome in non-small cell lung cancer

Annals of oncology, 2020-09, Vol.31, p.S713-S714

2020

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P2.04-76 Tumor Mutational Burden by TSO500 Next Generation Sequencing Panel and Clinical Outcome in Non-Small Cell Lung Cancer

Journal of thoracic oncology, 2019-10, Vol.14 (10), p.S738-S739

2019

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Detection and validation of copy number variation in X-linked mental retardation

Cytogenetic and genome research, 2008-01, Vol.123 (1-4), p.44-53

2008

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Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

Nature genetics, 2007-05, Vol.39 (5), p.593-595

2007

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Granulocyte chemotactic protein-2 and related CXC chemokines: from gene regulation to receptor usage

Journal of leukocyte biology, 1997-11, Vol.62 (5), p.563-569

1997

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A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients

Journal of medical genetics, 2003-01, Vol.40 (1), p.11-17

2003

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Tumour mutational burden ring trial: Evaluation of targeted next-generation sequencing platforms for implementation in clinical practice

Annals of oncology, 2019-12, Vol.30, p.xi10

2019

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Human Monocyte Chemotactic Protein-3 (MCP-3): Molecular Cloning of the cDNA and Comparison with Other Chemokines

Biochemical and biophysical research communications, 1993-03, Vol.191 (2), p.535-542

1993

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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

Human molecular genetics, 2005-07, Vol.14 (13), p.1795-1803

2005

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Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

The journal of histochemistry and cytochemistry, 2005-03, Vol.53 (3), p.413-422

2005

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CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior

Human molecular genetics, 2003-07, Vol.12 (13), p.1463-1474

2003

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Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

Human genetics, 2007-06, Vol.121 (5), p.539-547

2007

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Reliability of panel-based mutational signatures for immune-checkpoint-inhibition efficacy prediction in non-small cell lung cancer

Targeted next‐generation sequencing using a multigene panel in myeloid neoplasms: Implementation in clinical diagnostics

Gezamenlijke reflectie over ethische twijfel met CURA: een laagdrempelig instrument voor moreel beraad

Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map

Novel PORCN mutations in focal dermal hypoplasia

Sporadic male patients with intellectual disability: Contribution of X-chromosome copy number variants

Digitale werktuigkist met ethische overlegmethoden in de zorg

High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation

Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males

X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms

1037P Tumour mutational burden and HLA diversity by TruSight oncology 500 (TSO500) next generation sequencing panel and clinical outcome in non-small cell lung cancer

P2.04-76 Tumor Mutational Burden by TSO500 Next Generation Sequencing Panel and Clinical Outcome in Non-Small Cell Lung Cancer

Detection and validation of copy number variation in X-linked mental retardation

Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

Granulocyte chemotactic protein-2 and related CXC chemokines: from gene regulation to receptor usage

A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients

Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation

Tumour mutational burden ring trial: Evaluation of targeted next-generation sequencing platforms for implementation in clinical practice

Human Monocyte Chemotactic Protein-3 (MCP-3): Molecular Cloning of the cDNA and Comparison with Other Chemokines

Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior

Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome

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